The following data is part of a premarket notification filed by Arthrex, Inc. with the FDA for Arthrex Cannulated Interference Screw.
| Device ID | K915424 |
| 510k Number | K915424 |
| Device Name: | ARTHREX CANNULATED INTERFERENCE SCREW |
| Classification | Screw, Fixation, Bone |
| Applicant | ARTHREX, INC. 3050 NORTH HORSESHOE DR. SUITE 200 Naples, FL 33942 |
| Contact | Don Grafton |
| Correspondent | Don Grafton ARTHREX, INC. 3050 NORTH HORSESHOE DR. SUITE 200 Naples, FL 33942 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-12-02 |
| Decision Date | 1993-02-09 |